US2013023656A1PendingUtilityA1
Method for selective isolation and purification of nucleic acids
Est. expiryApr 8, 2030(~3.7 yrs left)· nominal 20-yr term from priority
C12N 15/1003C12N 15/101
34
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Claims
Abstract
The present invention relates to a gentle method for isolating and purifying nucleic acids from a biological cell comprising sample comprising at least DNA, RNA, and proteins, comprising at least the steps of 1. mixing the sample with a lysis buffer, 2. incubating the sample at a temperature within a range between 45° C. and 59° C. to obtain DNA as well as RNA or within a range between 60° C. and 70° C., to obtain DNA essentially free of RNA and 3. separating the nucleic acids from any contaminants.
Claims
exact text as granted — not AI-modified1 .- 6 . (canceled)
7 . A method for isolating and purifying nucleic acids from a cell comprising biological sample comprising at least DNA, RNA, and proteins, comprising:
(a) mixing the sample with a lysis buffer; (b) incubating the sample at a temperature
(i) within a range between 45° C. and 59° C. to obtain DNA as well as RNA, or
(ii) within a range between 60° C. and 70° C. to obtain DNA essentially free of RNA; and
(c) separating the nucleic acids essentially from any contaminants.
8 . The method according to claim 7 , wherein incubating in step (b) is carried out for at least 5 min.
9 . The method according to claim 7 , wherein incubating in step (b) is carried out for 10 to 80 min.
10 . The method according to claim 7 , wherein incubating in step (b) is carried out for 15 to 60 min.
11 . The method according to claim 7 , wherein the temperature range is from 50° C. to 58° C. for isolating a combination of DNA and RNA.
12 . The method according to claim 7 , wherein the temperature range is from 55° C. to 57° C. for isolating a combination of DNA and RNA.
13 . The method according to claim 7 , wherein the temperature range is from 61° C. to 65° C. for isolating DNA that is essentially free of RNA.
14 . The method according to claim 7 , wherein the temperature range is from 61° C. to 63° C. for isolating DNA that is essentially free of RNA.
15 . The method according to claim 7 , wherein the lysis buffer comprises an anionic surfactant.
16 . The method according to claim 7 , wherein the lysis buffer is essentially free of a chelating or complexing agent.
17 . The method according to claim 15 , wherein the lysis buffer has a pH in the range of pH 8 to 9.
18 . The method according to claim 16 , wherein the lysis buffer has a pH in the range of pH 8 to 9.Cited by (0)
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